Found: 22
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Impaired Angiogenic Potential of Human Placental Mesenchymal Stromal Cells in Intrauterine Growth Restriction.
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- Stem Cells Translational Medicine, 2016, v. 5, n. 4, p. 451, doi. 10.5966/sctm.2015-0155
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- Article
Preliminary Evidences of Safety and Efficacy of Flavonoids- and Omega 3-Based Compound for Muscular Dystrophies Treatment: A Randomized Double-Blind Placebo Controlled Pilot Clinical Trial.
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- Frontiers in Neurology, 2019, p. 1, doi. 10.3389/fneur.2019.00755
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- Article
Treatment with ROS detoxifying gold quantum clusters alleviates the functional decline in a mouse model of Friedreich ataxia.
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- Science Translational Medicine, 2021, v. 13, n. 607, p. 1, doi. 10.1126/scitranslmed.abe1633
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- Article
P(NIPAAM-co-HEMA) thermoresponsive hydrogels: an alternative approach for muscle cell sheet engineering.
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- Journal of Tissue Engineering & Regenerative Medicine, 2017, v. 11, n. 1, p. 187, doi. 10.1002/term.1898
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- Article
Effects of rituximab in two patients with dysferlin-deficient muscular dystrophy.
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- BMC Musculoskeletal Disorders, 2010, v. 11, p. 157, doi. 10.1186/1471-2474-11-157
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- Article
In Vivo Myogenic Potential of Human CD133<sup>+</sup> Muscle-derived Stem Cells: A Quantitative Study.
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- Molecular Therapy, 2009, v. 17, n. 10, p. 1771, doi. 10.1038/mt.2009.167
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- Article
Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy model.
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- Journal of Cell Biology, 2003, v. 162, n. 3, p. 511, doi. 10.1083/jcb.200210006
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- Article
Supplementation with a selective amino acid formula ameliorates muscular dystrophy in mdx mice.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-32613-w
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- Publication type:
- Article
Effective high-throughput isolation of enriched platelets and circulating pro-angiogenic cells to accelerate skin-wound healing.
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- Cellular & Molecular Life Sciences, 2022, v. 79, n. 5, p. 1, doi. 10.1007/s00018-022-04284-4
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- Article
Defective dystrophic thymus determines degenerative changes in skeletal muscle.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22305-x
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- Article
Novel insight into stem cell trafficking in dystrophic muscles.
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- International Journal of Nanomedicine, 2012, v. 7, p. 3059, doi. 10.2147/IJN.S30595
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- Article
Correlation of Circulating CD133+ Progenitor Subclasses with a Mild Phenotype in Duchenne Muscular Dystrophy Patients.
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- PLoS ONE, 2008, v. 3, n. 5, p. 1, doi. 10.1371/journal.pone.0002218
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- Publication type:
- Article
Full-length dysferlin expression driven by engineered human dystrophic blood derived CD133+ stem cells.
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- FEBS Journal, 2013, v. 280, n. 23, p. 6045, doi. 10.1111/febs.12523
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- Article
Perspectives of stem cell therapy in Duchenne muscular dystrophy.
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- FEBS Journal, 2013, v. 280, n. 17, p. 4251, doi. 10.1111/febs.12083
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- Publication type:
- Article
Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells.
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- Nature Cell Biology, 2007, v. 9, n. 3, p. 255, doi. 10.1038/ncb1542
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- Publication type:
- Article
Human skin‐derived stem cells migrate throughout forebrain and differentiate into astrocytes after injection into adult mouse brain.
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- Journal of Neuroscience Research, 2004, v. 77, n. 4, p. 475, doi. 10.1002/jnr.20151
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- Article
Stem Cell Tracking by Nanotechnologies.
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- International Journal of Molecular Sciences, 2010, v. 11, n. 3, p. 1070, doi. 10.3390/ijms11031070
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- Article
Human circulating AC133 + stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle.
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- Journal of Clinical Investigation, 2004, v. 114, n. 2, p. 182, doi. 10.1172/JCI200420325
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- Article
Human circulating AC133(+) stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle.
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- 2004
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- Publication type:
- journal article
Improvement of Endurance of DMD Animal Model Using Natural Polyphenols.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/680615
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- Publication type:
- Article
Autologous intramuscular transplantation of engineered satellite cells induces exosome-mediated systemic expression of Fukutin-related protein and rescues disease phenotype in a murine model of limb-girdle muscular dystrophy type 2I.
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- Human Molecular Genetics, 2017, v. 26, n. 19, p. 3682, doi. 10.1093/hmg/ddx252
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- Article
Blockade of IGF2R improves muscle regeneration and ameliorates Duchenne muscular dystrophy.
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- EMBO Molecular Medicine, 2020, v. 12, n. 1, p. N.PAG, doi. 10.15252/emmm.201911019
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- Publication type:
- Article